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Late-onset and long-lasting autoimmune neutropenia: an analysis from the Italian Neutropenia Registry.
Fioredda F, Rotulo GA, Farruggia P, Dagliano F, Pillon M, Trizzino A, Notarangelo L, Luti L, Lanza T, Terranova P, Lanciotti M, Ceccherini I, Grossi A, Porretti L, Verzegnassi F, Mastrodicasa E, Barone A, Russo G, Bonanomi S, Boscarol G, Finocchi A, Veltroni M, Ramenghi U, Onofrillo D, Martire B, Ghilardi R, Giordano P, Ladogana S, Marra N, Zanardi S, Beier F, Miano M, Dufour C. Fioredda F, et al. Among authors: lanza t. Blood Adv. 2020 Nov 24;4(22):5644-5649. doi: 10.1182/bloodadvances.2020002793. Blood Adv. 2020. PMID: 33206964 Free PMC article.
Autoimmune neutropenia of infancy: Data from the Italian neutropenia registry.
Farruggia P, Fioredda F, Puccio G, Porretti L, Lanza T, Ramenghi U, Ferro F, Macaluso A, Barone A, Bonanomi S, Caruso S, Casazza G, Davitto M, Ghilardi R, Ladogana S, Mandaglio R, Marra N, Martire B, Mastrodicasa E, Dora Notarangelo L, Onofrillo D, Robustelli G, Russo G, Trizzino A, Tucci F, Pillon M, Dufour C. Farruggia P, et al. Among authors: lanza t. Am J Hematol. 2015 Dec;90(12):E221-2. doi: 10.1002/ajh.24187. Epub 2015 Oct 6. Am J Hematol. 2015. PMID: 26361081 Free article. No abstract available.
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry.
Farruggia P, Puccio G, Fioredda F, Lanza T, Porretti L, Ramenghi U, Barone A, Bonanomi S, Finocchi A, Ghilardi R, Ladogana S, Marra N, Martire B, Notarangelo LD, Onofrillo D, Pillon M, Russo G, Lo Valvo L, Serafinelli J, Tucci F, Zunica F, Verzegnassi F, Dufour C. Farruggia P, et al. Among authors: lanza t. Am J Hematol. 2017 Sep;92(9):E546-E549. doi: 10.1002/ajh.24803. Epub 2017 Jul 7. Am J Hematol. 2017. PMID: 28567966 Free article. No abstract available.
Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry.
Farruggia P, Fioredda F, Puccio G, Onofrillo D, Russo G, Barone A, Bonanomi S, Boscarol G, Finocchi A, Ghilardi R, Giordano P, Ladogana S, Lassandro G, Luti L, Lanza T, Mandaglio R, Marra N, Martire B, Mastrodicasa E, Motta M, Notarangelo LD, Pillon M, Porretti L, Serafinelli J, Trizzino A, Tucci F, Veltroni M, Verzegnassi F, Ramenghi U, Dufour C. Farruggia P, et al. Among authors: lanza t. Am J Hematol. 2019 Feb;94(2):216-222. doi: 10.1002/ajh.25353. Epub 2018 Dec 18. Am J Hematol. 2019. PMID: 30456824 Free article.
Pegfilgrastim in children with severe congenital neutropenia.
Fioredda F, Calvillo M, Lanciotti M, Lanza T, Giunti L, Castagnola E, Lorenzi I, Tonelli R, Ghezzi P, Dufour C. Fioredda F, et al. Among authors: lanza t. Pediatr Blood Cancer. 2010 Mar;54(3):465-7. doi: 10.1002/pbc.22350. Pediatr Blood Cancer. 2010. PMID: 19927291
Poikiloderma with neutropenia: a case report and review of the literature.
Farruggia P, Indaco S, Dufour C, Lanza T, Mosa C, Macaluso A, Milioto M, D'Angelo P, Lanciotti M. Farruggia P, et al. Among authors: lanza t. J Pediatr Hematol Oncol. 2014 May;36(4):297-300. doi: 10.1097/MPH.0b013e31829f35e7. J Pediatr Hematol Oncol. 2014. PMID: 23823120 Review.
Unusual Late-onset Enteropathy in a Patient With Lipopolysaccharide-responsive Beige-like Anchor Protein Deficiency.
Maggiore R, Grossi A, Fioredda F, Palmisani E, Terranova P, Cappelli E, Lanza T, Pierri F, Guardo D, Calvillo M, Micalizzi C, Beccaria A, Coccia MC, Arrigo S, Dufour C, Ceccherini I, Miano M. Maggiore R, et al. Among authors: lanza t. J Pediatr Hematol Oncol. 2020 Nov;42(8):e768-e771. doi: 10.1097/MPH.0000000000001708. J Pediatr Hematol Oncol. 2020. PMID: 31876783
Genetic screening of children with marrow failure. The role of primary Immunodeficiencies.
Miano M, Grossi A, Dell'Orso G, Lanciotti M, Fioredda F, Palmisani E, Lanza T, Guardo D, Beccaria A, Ravera S, Cossu V, Terranova P, Giona F, Santopietro M, Cappelli E, Ceccherini I, Dufour C. Miano M, et al. Among authors: lanza t. Am J Hematol. 2021 Sep 1;96(9):1077-1086. doi: 10.1002/ajh.26242. Epub 2021 Jun 2. Am J Hematol. 2021. PMID: 34000087 Free article.
FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene.
Miano M, Cappelli E, Pezzulla A, Venè R, Grossi A, Terranova P, Palmisani E, Maggiore R, Guardo D, Lanza T, Calvillo M, Micalizzi C, Pierri F, Vernarecci C, Beccaria A, Corsolini F, Lanciotti M, Russo G, Ceccherini I, Dufour C, Fioredda F. Miano M, et al. Among authors: lanza t. Br J Haematol. 2019 Nov;187(4):502-508. doi: 10.1111/bjh.16098. Epub 2019 Jul 15. Br J Haematol. 2019. PMID: 31309545 Free article.
85 results